United States · FDA National Drug Code directory
Tramadol Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63187-063_59d339c1-6ad2-4407-ac41-74e5f4dda6e8
- Product NDC
- 63187-063
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101115
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, COATED in 1 BOTTLE (63187-063-15) · 63187-063-15
- 20 TABLET, COATED in 1 BOTTLE (63187-063-20) · 63187-063-20
- 30 TABLET, COATED in 1 BOTTLE (63187-063-30) · 63187-063-30
- 40 TABLET, COATED in 1 BOTTLE (63187-063-40) · 63187-063-40
- 60 TABLET, COATED in 1 BOTTLE (63187-063-60) · 63187-063-60
- 240 TABLET, COATED in 1 BOTTLE (63187-063-64) · 63187-063-64
- 120 TABLET, COATED in 1 BOTTLE (63187-063-72) · 63187-063-72
- 180 TABLET, COATED in 1 BOTTLE (63187-063-78) · 63187-063-78
- 90 TABLET, COATED in 1 BOTTLE (63187-063-90) · 63187-063-90
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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